Tag | Content |
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EnhancerAtlas ID | HS133-22922 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:127997480-127999970 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr3:127998593-127998604 | TTCTGTGGTTT | + | 6.32 | ZNF263 | MA0528.1 | chr3:127999070-127999091 | GGAGGAGTGAGGGAAAGTGGA | + | 6.42 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41945 | chr3:127999233-128002747 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I128277 | chr3 | 127996830 | 128000288 |
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Enhancer Sequence | TAAAAAGCAA GCTTCAGCTG TTTCATCTAA AGTTATAATT CCGATGCTTT AAAGGCTCCC 60 AACCCTCTTC TTGTTCATGG TGGGGGAGCC TTCCTAGTTG TGAAAGGGTC TGAGTGGCTC 120 CAGCTTTGGC ATATTAGGGT GCAGGGGAGG GTATTTCTAG GGACACTCTG GGAGAAGCTG 180 CCCAGCCTGC ATGGTGCTAG TGCCAGTCTG CAAAATCTCC AGGTAATAGA GAGGGCAGGC 240 CCCTGCCCAC CCCCTTGCAG CCTCCAATGC TGCTGCTGTG GCAGCTGCTG CTGCGAAACA 300 AACCAGGGTG ACTGGGCGGA AGGTCAGGAG TTTAAGAGCT TGTTTGATTC AAAACTAGGC 360 TAAAAGACAG GAGGGGAGTG AGCTGGTTTT CTGTGTGGAT CCTGGTATTT TCCTTTGAGT 420 TGGGGAGGAG AATGGTGGGG CAGGGAGGGA AGGCCGGCCG CCAGAGGGAA CGCTGCCAAG 480 CAGAGCGCAG CTAATGTGAA CCATACGGCG GCGGCGTTGG GCAGTGGCGG CCATCTCCCG 540 CCCAGCTTAG TACAGCCCTT ACTGCGGGCA GGGGTGCAGA CAGGCAGGAA GGCAGCTCGG 600 GCTGTGCGGC CACTTAACCC TTCCAGTGCT GAACTACAAG CAGGGCTCCT TCACCTCAGC 660 ACATTGATGT TTCAGCCAAT AATCCTCTGT CCTGGGCACT GTAGATGTCT AGCAGCATCC 720 CTGGCCTCTA CCCACTAGAT GCCAATAGCA CCCTCTCCCA GCTGTGATGA CCACAAGTGT 780 CTGCAGACAT TCTAAATGCC TCCTGGGGGG AAATTATCCC TGGCGGAGAA CCAGTGGCCT 840 AGAACAGGCG GCCCCCTCAG CTGCTGGGCC TGCCTGGACT CTGATGGGCC TGCACCCTTC 900 AGGGGCCCTG CCCCAGACAC ACCACATCCA TGTTTGGAGT GCTGCCTGGG GCTGAGCATG 960 TGGGGGTCGT TTTCCCATGA AGCAGGCAGC CATAGGGTCA GAGGGGAGAC GAGACCTACC 1020 CAGAGTTGTA TGCCAGTAGG AGCCAGGGTC CAGGATTGGT GTTGCTCCAC ACATTCCCTG 1080 TCCCCCTGCT CCCAGGCATG GCCCCCATTC AGTTTCTGTG GTTTTAAGTG GGAGGTGTGC 1140 AGCCTGCCCC TGACTGGCTT CCTGGGGGGA CTAATTCCTA TGCCAGCCTT CTCTGCCTAT 1200 TCAACATGCA GTTGCCCAAG GGAACATGGC ACGGGTGTTT ACCACACTGT TCTTATACCA 1260 AGAGTCAGTG CACACGAGCT CAGTGTCCAG CGGTGGGTCT GGTTCTCTAA ACCGTGCGAT 1320 ACCACGTGCC CATCGAACAC GATGGTGCAG ATCTATGTGG AAAGACCACC ATTAGAATCA 1380 TCAGATCCGC GAGGACAGAG ACTTTTGTCA GTCATGTTCC TGGGCCCTTA ATAAATGTCC 1440 TGTGAATAAA TAAAATGCTA ATTGCAAAAC CAAATCTCAA TATGTATGAT TTGGTCCCAT 1500 TATGTAGGAA AACTGTCTGC ATATGTTTGT ATACAAATGC ATCAAAAAAT CTGGAAGGAG 1560 ACAGCAAACT GAGAACAGTG GCTGCATCTT GGAGGAGTGA GGGAAAGTGG AATTTAGAGG 1620 GCTGAAAGAG AGCTTTCATG TTTCAGTCTA TTTAATTGGT GTTTAAATCT TTTACAACGA 1680 GCTGGTATTC ATCTGTTTCT TGTGTGGCTT TTATGAAAGA AAAAATATAA AGAACTGGAA 1740 AAAGAGCAAC TTTTGTTCTG TCCTTCCCTG TTCTCTCTCA CCTCCCTTGT GCCCTCACTC 1800 GGCTTTGGCC TGGAAAGTCC GTTCTCTGCT GGGGAGGCCT CTGTGTAGGG AGCCCAGGGG 1860 TCTGGCCTGG CACTGTTCTG CTGAGGGCCA CCTCCTTTTC AGAAAGCTGG AATGGGCCCC 1920 TCCTCCTGGC CCCTGTGCAT GGATGCCACT ACTGGGCTTC CCTGTCCTCC CTGAGCCCTC 1980 CAGGAGCTCC CTGGCACCAG TTGGCATTTG CCCTCCACAT GGCAGTGCCC TCCTTGCCTC 2040 TGTACGGTCT TCCCTCTGGG CCCTCAAGCT GGGGCTCGCA CAGCAAGCGG CAGCCTCTAC 2100 TTTATTGGGG AAGCTCTGGG CACCAACCCT CACCCCCTTC TCCTTCACTA GCCGCCCTGC 2160 ATGATTCCCC TCCCAGCTGT TTCTGCTCAT TTCTCTGAAG TTTTCAGCCC TTTTTCTCCT 2220 ACTCACTGTT TTTTTTCCCC TCCACACTCC CCTCCTCGGA GATGCAGCCT GAGGCTGAGG 2280 CCGCATTGTT TGGTGACCTT CCCTGCTGTC CCAGGCTGCC TGCACATTAT CATATACAAA 2340 TACTTTCGTC CCTTTCACAG CAGCTGCCAT CTTTGCTGAC TCTTTCATTA CCCCCTCCGC 2400 TTCAGCCTAG GCAAACAGGT CTCTGCAGGT GGTGACAGTG ATAATTTCCT GTCCATGGAA 2460 AGCCTGCTCT CCCCGCAGCA CCATAGCAGG 2490
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